线粒体钙离子通道(MCUC)介导的钙信号网络系统图。

Hilda Delgado de la Herran,Denis Vecellio Reane,Yiming Cheng,Máté Katona,Fabian Hosp,Elisa Greotti,Jennifer Wettmarshausen,Maria Patron,Hermine Mohr,Natalia Prudente de Mello,Margarita Chudenkova,Matteo Gorza,Safal Walia,Michael Sheng-Fu Feng,Anja Leimpek,Dirk Mielenz,Natalia S Pellegata,Thomas Langer,György Hajnóczky,Matthias Mann,Marta Murgia,Fabiana Perocchi
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引用次数: 0

摘要

线粒体钙离子通道(MCUC)介导线粒体钙离子进入,调节能量代谢和细胞死亡。虽然已经确定了几种 MCUC 成分,但线粒体钙信号网络的分子基础及其在单向传输通道活性变化时的重塑尚未得到评估。在这里,我们绘制了线粒体钙摄取在静息条件下和长期丧失或增加时的 MCUC 相互作用组图谱。我们发现了 89 个高置信度的相互作用体,它们将 MCUC 与多个线粒体复合物和途径联系起来,其中一半与人类疾病相关。作为概念证明,我们验证了线粒体膜间空间蛋白 EFHD1 是 MCUC 亚基 MCU、EMRE 和 MCUB 的结合伙伴。我们进一步证明了 EFHD1 对钙吸收的抑制作用依赖于 MICU1。接下来,我们通过分析敲除 EMRE、MCUB、MICU1 或 MICU2 后 MCU 的相互作用组,系统地研究了线粒体钙失调的补偿机制和功能性后果。沉默EMRE会降低MCU的相互关联性,而MCUB功能缺失则会导致更广泛的相互作用网络。我们的研究为深入了解线粒体钙信号转导的参与者和机制及其与人类疾病的相关性提供了全面、高置信度的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Systematic mapping of mitochondrial calcium uniporter channel (MCUC)-mediated calcium signaling networks.
The mitochondrial calcium uniporter channel (MCUC) mediates mitochondrial calcium entry, regulating energy metabolism and cell death. Although several MCUC components have been identified, the molecular basis of mitochondrial calcium signaling networks and their remodeling upon changes in uniporter activity have not been assessed. Here, we map the MCUC interactome under resting conditions and upon chronic loss or gain of mitochondrial calcium uptake. We identify 89 high-confidence interactors that link MCUC to several mitochondrial complexes and pathways, half of which are associated with human disease. As a proof-of-concept, we validate the mitochondrial intermembrane space protein EFHD1 as a binding partner of the MCUC subunits MCU, EMRE, and MCUB. We further show a MICU1-dependent inhibitory effect of EFHD1 on calcium uptake. Next, we systematically survey compensatory mechanisms and functional consequences of mitochondrial calcium dyshomeostasis by analyzing the MCU interactome upon EMRE, MCUB, MICU1, or MICU2 knockdown. While silencing EMRE reduces MCU interconnectivity, MCUB loss-of-function leads to a wider interaction network. Our study provides a comprehensive and high-confidence resource to gain insights into players and mechanisms regulating mitochondrial calcium signaling and their relevance in human diseases.
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